Stereo- and regio-control of 1,3-dipolar cycloaddition reactions by the aid of Lewis acid catalysts - Nitrone and aci-nitro compound cycloadditions

Authors
Citation
S. Kanemasa, Stereo- and regio-control of 1,3-dipolar cycloaddition reactions by the aid of Lewis acid catalysts - Nitrone and aci-nitro compound cycloadditions, NIP KAG KAI, (3), 2000, pp. 155-165
Citations number
90
Categorie Soggetti
Chemistry
Journal title
NIPPON KAGAKU KAISHI
ISSN journal
03694577 → ACNP
Issue
3
Year of publication
2000
Pages
155 - 165
Database
ISI
SICI code
0369-4577(200003):3<155:SARO1C>2.0.ZU;2-8
Abstract
Much attention is now focussed on the stereo- and regiocontrol of 1,3-dipol ar cycloaddition reactions by the aid of a Lewis acid catalyst. The report of catalyzed asymmetric nitrone cycloadditions has triggered the accelerati on of research development of this field. This review describes the Lewis a cid-catalyzed nitrone cycloadditions to electron-deficient alkenes, the Lew is acid-catalyzed nitrone cycloadditions to electron-rich alkenes such as a llylic alcohols, and asymmetric nitrone and aci-nitro compound cycloadditio ns to electron-deficient alkenes catalyzed by DBFOX/Ph metal complexes.